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首页> 外文期刊>Diabetes, obesity & metabolism >Rates of myocardial infarction and stroke in patients initiating treatment with SGLT SGLT 2‐inhibitors versus other glucose‐lowering agents in real‐world clinical practice: R R esults from the CVD‐REAL CVD‐REAL study
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Rates of myocardial infarction and stroke in patients initiating treatment with SGLT SGLT 2‐inhibitors versus other glucose‐lowering agents in real‐world clinical practice: R R esults from the CVD‐REAL CVD‐REAL study

机译:用SGLT SGLT 2抑制剂的患者对患者进行心肌梗死和中风的速率与现实世界临床实践中的其他葡萄糖降低剂:来自CVD-Real CVD-Real研究的results

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The multinational, observational CVD‐REAL study recently showed that initiation of sodium‐glucose co‐transporter‐2 inhibitors (SGLT‐2i) was associated with significantly lower rates of death and heart failure vs other glucose‐lowering drugs (oGLDs). This sub‐analysis of the CVD‐REAL study sought to determine the association between initiation of SGLT‐2i vs oGLDs and rates of myocardial infarction (MI) and stroke. Medical records, claims and national registers from the USA, Sweden, Norway and Denmark were used to identify patients with T2D who newly initiated treatment with SGLT‐2i (canagliflozin, dapagliflozin or empagliflozin) or oGLDs. A non‐parsimonious propensity score was developed within each country to predict initiation of SGLT‐2i, and patients were matched 1:1 in the treatment groups. Pooled hazard ratios (HRs) and 95% CIs were generated using Cox regression models. Overall, 205?160 patients were included. In the intent‐to‐treat analysis, over 188?551 and 188?678 person‐years of follow‐up (MI and stroke, respectively), there were 1077 MI and 968 stroke events. Initiation of SGLT‐2i vs oGLD was associated with a modestly lower risk of MI and stroke (MI: HR, 0.85; 95%CI, 0.72‐1.00; P ?=?.05; Stroke: HR, 0.83; 95% CI, 0.71‐0.97; P ?=?.02). These findings complement the results of the cardiovascular outcomes trials, and offer additional reassurance with regard to the cardiovascular effects of SGLT‐2i, specifically as it relates to ischaemic events.
机译:跨国公司,观察性CVD-Real研究最近显示钠葡萄糖共转运蛋白-2抑制剂(SGLT-2I)的起始与其他葡萄糖降低药物(OGLD)的死亡和心力衰竭率明显降低。这种CVD实际研究的次分析试图确定SGLT-2I与OGLD和心肌梗死率(MI)和中风的开始之间的关联。来自美国,瑞典,挪威和丹麦的医疗记录,索赔和国家登记册用于鉴定与SGLT-2I(蜜胶,Dapagliflozin或Empagliflozin)或OGLD的新发起治疗的T2D患者。在每个国家内开发出一个非分类的倾向评分以预测SGLT-2I的开始,并且患者在治疗组中匹配1:1。使用COX回归模型产生汇集危险比(HRS)和95%CIS。总体而言,包括205例160名患者。在意图分析中,超过188年?551和188?678人的后续随访(分别),有1077英里和968例卒中事件。 SGLT-2I对OGLD的开始与MI和中风的风险适度较低(MI:HR,0.85; 95%CI,0.72-1.00; P?=Δ.05;中风:HR,0.83; 95%CI, 0.71-0.97; p?= 02)。这些发现补充了心血管成果试验的结果,并提供了对SGLT-2i的心血管作用的额外保证,具体如此,因为它涉及缺血事件。

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